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FDA 510(k)

CALCIUM PHOSPHATE GRANULAR BONE VOID FILLER

K-Number: K011531 · 2002-09-06

ApplicantBiomet, Inc.
Decision Date2002-09-06
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CALCIUM PHOSPHATE GRANULAR BONE VOID FILLER is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2002-09-06 under 510(k) number K011531. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CALCIUM PHOSPHATE GRANULAR BONE VOID FILLER?

CALCIUM PHOSPHATE GRANULAR BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 2002-09-06. The listed applicant is Biomet, Inc.. The 510(k) number is K011531.

When did CALCIUM PHOSPHATE GRANULAR BONE VOID FILLER receive FDA 510(k) clearance?

CALCIUM PHOSPHATE GRANULAR BONE VOID FILLER received FDA 510(k) clearance on 2002-09-06, under 510(k) number K011531.

Who is the listed applicant for CALCIUM PHOSPHATE GRANULAR BONE VOID FILLER?

The FDA 510(k) record lists Biomet, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CALCIUM PHOSPHATE GRANULAR BONE VOID FILLER?

The FDA product code for CALCIUM PHOSPHATE GRANULAR BONE VOID FILLER is MQV.

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Related Devices (Code: MQV)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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